Evidence map›Paper›PMID 36864824›Full record

ArticleTransplant infectious disease : an official journal of the Transplantation Society2023

Phage therapy in a lung transplant recipient with cystic fibrosis infected with multidrug-resistant Burkholderia multivorans.

Ghady Haidar, Benjamin K Chan, Shu-Ting Cho, Kailey Hughes Kramer, Hayley R Nordstrom, Nathan R Wallace, Madison E Stellfox, Mische Holland, Ellen G Kline, Jennifer M Kozar and 6 more

Registry-linked trialOpen access · hybridAbstract readCase Reports
In one paragraph

Article in Transplant infectious disease : an official journal of the Transplantation Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07275905 (A Phase 1, Open-label, Randomized, Pilot and Feasibility Trial to Evaluate the Safety and Tolerability of the Achromobacter-targeting Bacteriophage Cocktail, AchromoPhage, Among Persons With Cystic Fibrosis and Chronic Achromobacter Lung Infections), which is not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
8.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07275905 phase1recruitingnot on this mapstarted 2026, after this paper: background citation

A Phase 1, Open-label, Randomized, Pilot and Feasibility Trial to Evaluate the Safety and Tolerability of the Achromobacter-targeting Bacteriophage Cocktail, AchromoPhage, Among Persons With Cystic Fibrosis and Chronic Achromobacter Lung Infections: The AchromoPhage Trial

TypeinterventionalSponsorGhady HaidarRan2026 to 2028Enrolled12ConditionsCystic Fibrosis (CF), Achromobacter InfectionArmsAchromoPhage
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Colony morphotype variation inJournal of bacteriology · 2025
    Review
  6. Review
  7. Pulmonary microbial spectrum ofFrontiers in medicine · 2025
    Article
  8. Annals of medicine · 2024
    Review
  9. Review
  10. Phage therapy: breathing new tactics into lower respiratory tract infection treatments.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  11. Article
  12. Article
  13. Harnessing the diversity ofbioRxiv : the preprint server for biology · 2024
    Article
  14. Review
  15. Review
  16. Phage therapy to treat cystic fibrosisFrontiers in microbiology · 2024
    Review
  17. Article
  18. Bacteriophage steering ofJournal of bacteriology · 2023
    Article
  19. Automating Predictive Phage Therapy Pharmacology.Antibiotics (Basel, Switzerland) · 2023
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 1 country.

Ghady HaidarDivision of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0003-0634-8211
Benjamin K ChanDepartment of Ecology and Evolutionary Biology, and Yale Center for Phage Biology and Therapy, Yale University, New Haven, Connecticut, USA.
Shu-Ting ChoDivision of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0003-2140-5165
Kailey Hughes KramerDivision of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-7028-6062
Hayley R NordstromDivision of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Nathan R WallaceDivision of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Madison E StellfoxDivision of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-1478-5190
Mische HollandDivision of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-4917-9211
Ellen G KlineDivision of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Jennifer M KozarInvestigational Drug Service, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Silpa D KilaruDivision of Pulmonary, Allergy, and Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Joseph M PilewskiDivision of Pulmonary, Allergy, and Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-0893-1155
John J LiPumaDepartment of Pediatrics, University of Michigan School of Medicine, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0003-4033-7794
Vaughn S CooperDepartment of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0001-7726-0765
Ryan K ShieldsDivision of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0001-9794-5665
Daria Van TyneDivision of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0001-7284-0103
University of Pittsburgh · USUniversity of Michigan · USUniversity of Pittsburgh Medical Center · USYale University · US

Funding

University of Pittsburgh Training Program in Antimicrobial ResistanceT32AI138954 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HARRISON, LEE H · 2019 to 2023
$971k
The Gut Microbiome in Carbapenem-Resistant Enterobacteriaceae Colonization, Persistence, Infection, and Tolerance after Lung or Liver TransplantationK23AI154546 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HAIDAR, GHADY · 2021 to 2025
$896k
Cystic Fibrosis Foundation BOMBER19R0Cystic Fibrosis Foundation VANTYN21GODepartment of Medicine at the University of Pittsburgh School of MedicineNational Institute of Allergy and Infectious Diseases K23AI154546NIAID NIH HHS K23 AI154546NIAID NIH HHS T32 AI138954
6 · The paper itself

Abstract

backgroundThere is increased interest in bacteriophage (phage) therapy to treat infections caused by antibiotic-resistant bacteria. A lung transplant recipient with cystic fibrosis and Burkholderia multivorans infection was treated with inhaled phage therapy for 7 days before she died.

methodsPhages were given via nebulization through the mechanical ventilation circuit. Remnant respiratory specimens and serum were collected. We quantified phage and bacterial deoxyribonucleic acid (DNA) using quantitative polymerase chain reaction, and tested phage neutralization in the presence of patient serum. We performed whole genome sequencing and antibiotic and phage susceptibility testing on 15 B. multivorans isolates. Finally, we extracted lipopolysaccharide (LPS) from two isolates and visualized their LPS using gel electrophoresis.

resultsPhage therapy was temporally followed by a temporary improvement in leukocytosis and hemodynamics, followed by worsening leukocytosis on day 5, deterioration on day 7, and death on day 8. We detected phage DNA in respiratory samples after 6 days of nebulized phage therapy. Bacterial DNA in respiratory samples decreased over time, and no serum neutralization was detected. Isolates collected between 2001 and 2020 were closely related but differed in their antibiotic and phage susceptibility profiles. Early isolates were not susceptible to the phage used for therapy, while later isolates, including two isolates collected during phage therapy, were susceptible. Susceptibility to the phage used for therapy was correlated with differences in O-antigen profiles of an early versus a late isolate.

conclusionsThis case of clinical failure of nebulized phage therapy highlights the limitations, unknowns, and challenges of phage therapy for resistant infections.

Indexed as

Burkholderia cepacia complexBurkholderia InfectionsCystic FibrosisPhage TherapyAdultAnti-Bacterial AgentsBurkholderiaDNAFatal OutcomeFemaleHumansLeukocytosisLipopolysaccharidesLungTransplant RecipientsAnti-Bacterial AgentsDNALipopolysaccharidesantibiotic resistanceBurkholderiacystic fibrosisphage therapy

Identifiers

PMID36864824
PMCPMC10085838
OpenAlexW4323035936

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.